Job Description

(a) Assist in QC stability testing, prepare and maintain stability records and summaries.
(b) Involve in training and transfer of methods to and from QC
(c) Modify and validate analytical procedures to meet QC's needs
(d) Support design and development of experimental protocols, SOP's, etc., consistent with GMP Standards
(e) Execute special projects on analytical and instrument problem solving.
(f) Conduct all quality QC chemical tests
(g) Adapt, maintain and operate analytical instrumentation
(h) Involve in procedure review and propose modifications and updates
(i) Ensure work environment is clean and safe complying with safety and pharmaceutical regulation.
(j) Contribute to industrial, R&D qualification and validation activities and support routine maintenance
(k) Conduct various analytical testing procedures as per manufacturing/QC SOPs

Job Type: Full-time

Pay: ?20,000.00 - ?25,403.04 per month

Benefits:

• Health insurance

Schedule:

• Day shift

Supplemental Pay:

• Performance bonus

Experience:

• total work: 1 year (Required)

Work Location: In person